Efficient synthesis of 3-aminoquinolines has been demonstrated from readily accessible N-sulfonyl-1,2,3-triazoles and o-acylaniline derivatives. This transformation involves the generation of C-C and C-N bonds through insertion of rhodium azavinyl carbenoid into a N-H bond followed by cyclization and aromatization. The important features include good functional group tolerance, synthesis of indoloquinoline, and isolation of N-H-inserted product, a potential intermediate.
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